Clinical presentation of Crohn's disease. Association between familial disease, smoking, disease phenotype, extraintestinal manifestations and need for surgery [PDF]
Background/Aims: Recent molecular data suggest that genetic factors may underlie the disease heterogeneity observed in Crohn's disease (CD). It was also suggested that familial inflammatory bowel disease (IBD) is a homogenous subgroup, phenotypically ...
Gasztonyi, Beáta +16 more
core +2 more sources
Giant retroperitoneal lipoma in a child misdiagnosed as Hirschsprung's disease
Retroperitoneal lipomas have remained the essentially rare tumors seen in clinical practice. The tumors are rarer in children, with very few reported cases in surgical literature worldwide.
Aditya Pratap Singh +3 more
doaj +1 more source
The Swedish National Pediatric Cataract Register (PECARE): Coexisting systemic disorders 2007–2023
Abstract Purpose To analyse the frequency and type of coexisting systemic disorders in children operated on for cataract in Sweden. Methods Data were retrieved from the Swedish National Pediatric Cataract Register (PECARE) for children operated between January 1, 2007, and December 31, 2023 (n = 975), including follow‐ups at age 1, 2, 5 and 10 ...
David Wackerberg +9 more
wiley +1 more source
Chronic Intestinal Failure During the Neonatal Period Related to Height at Five Years of Age
ABSTRACT Aim To clarify if children with chronic intestinal failure during the neonatal period had a different height at 5 years of age compared to standardised Swedish growth charts. Methods This retrospective cohort study of children with chronic intestinal failure during the neonatal period in Gothenburg between 2004 and 2018.
Johanna Mårtenson +5 more
wiley +1 more source
Conditions that mimic Hirschsprung’s disease, but that are not Hirschsprung’s disease
Hirschsprung’s disease (HSCR) is widely recognized in pediatric surgery. This condition has been elucidated, and therapeutic approaches have been developed. However, even when ganglion cells are present in the rectum, some patients still experience symptoms such as bowel obstruction, intestinal dilatation, and chronic constipation, which are similar to
Shun Onishi, Satoshi Ieiri
openaire +2 more sources
Hirschsprung’s disease in adults
Hirschsprung?s disease is the malformation of the hindgut characterized by the absence of intramural ganglion cells in the submucosal and myenteric plexuses and manifested by megacolon. Congenital character of this disease stipulates its belonging in general to the scope of activity of the pediatric clinics.
G I, Vorobyov +2 more
openaire +3 more sources
Fifth disease (slapped cheek syndrome)
What is fifth disease Fifth disease, which is also known as ?slapped cheek syndrome? or erythema infectiosum is a common viral infection caused by parvovirus B19.
Centre for Disease Control
core
Case Report: Adult Hirschsprung's Disease
BACKGROUND: Hirschsprung’s disease (HD) remains the most common condition to cause low functional intestinal obstruction in children. It is caused by the failed migration of colonic ganglion cells during gestation.
Kevin Wortman +2 more
doaj
Outcome of transanal endorectal pull-through in patients with hirschsprung's disease
Background: Transanal endorectal pull-through (TERPT) has become one of the preferred treatments for Hirschsprung's disease (HD) in our setting. This report aims to evaluate the current outcome of TERPT in the setting.
Tunde Talib Sholadoye +4 more
doaj +1 more source
Water-related disease outbreaks surveillance /
Title from cover.Mode of access: Internet.Vol.
Centers for Disease Control (U.S.) +1 more
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